Evolution of lmiRNAs and their targets from MITEs for rice adaptation

Abstract

Twenty‐four nucleotide long microRNAs (lmiRNAs) direct DNA methylation at target genes and regulate their transcription. The evolutionary origin of lmiRNAs and the range of lmiRNA‐mediated regulation remain obscure. Here, we reannotated lmiRNAs and their targets in rice by applying stringent criteria. We found that the majority of lmiRNAs are derived from Miniature Inverted‐repeat Transposable Elements (MITEs) and most sites targeted by MITE‐derived lmiRNAs reside within MITEs, suggesting co‐evolution of lmiRNAs and their targets through MITE amplification. lmiRNAs undergo dynamically changes under stress conditions and the genes targeted by lmiRNAs show an enrichment for stress‐responsive genes, suggesting that lmiRNAs are widely involved in plant responses to stresses. We constructed the evolutionary histories of lmiRNAs and their targets. Nearly half of lmiRNAs emerged before or when the AA genome was diverged, while the emergence of lmiRNA targets coincided with or followed the emergence of lmiRNAs. Furthermore, we found that the sequences of a lmiRNA target site underwent variations, coincident with the divergence of rice accessions and the distribution of rice accessions in different geographical locations and climatic conditions. Our findings highlight MITEs as an important origin of lmiRNAs and suggest that the evolution of lmiRNA‐target regulatory modules may contribute to rice adaptation to environmental changes.

Peptidyl-prolyl isomerase Cyclophilin71 promotes SERRATE phase separation and miRNA processing in Arabidopsis

“…MicroRNAs (miRNAs) are 21–24-nucleotide (nt) small RNAs that play important regulatory roles in plant development and responses to biotic and abiotic stresses ( 1 , 2 ). 21-nt miRNAs are associated with ARGONAUTE 1 (AGO1) to down-regulate target gene expression through mRNA cleavage and/or translation inhibition ( 3 ), whereas 24-nt long miRNAs are associated with AGO4 to repress target gene transcription through DNA methylation ( 4 , 5 ).…”